Isopropamide
This anticholinergic drug reduces secretions from glands and relaxes smooth muscle in the digestive tract, making it useful for treating peptic ulcers and irritable bowel syndrome. It works by blocking muscarinic receptors that stimulate secretions and gut motility.
Peso molecular
353,5000 g/mol
LogP
4,30
TPSA
43,10 Ų
Regla de cinco de Lipinski
Cumple
Mecanismo de acción
Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.
Estructura 2D
Cite this structure
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SMILES
CC(C)[N+](C)(CCC(C(N)=O)(c1ccccc1)c1ccccc1)C(C)C
InChI
InChI=1S/C23H32N2O/c1-18(2)25(5,19(3)4)17-16-23(22(24)26,20-12-8-6-9-13-20)21-14-10-7-11-15-21/h6-15,18-19H,16-17H2,1-5H3,(H-,24,26)/p+1
Molecular Formula
C23H33N2O+
HBD / HBA
1 / 1
Enlaces Rotables
8
Átomos Pesados
26
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Preguntas frecuentes
This anticholinergic drug reduces secretions from glands and relaxes smooth muscle in the digestive tract, making it useful for treating peptic ulcers and irritable bowel syndrome. It works by blocking muscarinic receptors that stimulate secretions and gut motility.
Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.
Yes, Isopropamide is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201232. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3775. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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